Can vessel
ID
Bron
Verkorte titel
Aandoening
Glioblastoma, Glioblastoom
Brain tumour, hersentumor
Ondersteuning
University of Groningen (MD/PhD grant: B.R.J. van Dijken, Mandema grant: A. van der Hoorn)
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary outcome is to establish the practicability abd diagnostic accuracy of VAI-MRI for the treatment evaluation of glioblastoma.
Achtergrond van het onderzoek
Glioblastomas (GBM) are the most malignant brain tumours with low survival rates. Treatment failure causes this tumour to inevitably recur, making close monitoring of GBM patients essential. The gold standard for follow-up is anatomical MR imaging based on contrast enhancement. However, this imaging method is hindered by pseudo-progression which can resemble true tumour progression, but is in fact due to treatment effects.
Functional imaging methods have been employed to overcome the limitations of anatomical MRI by measuring biological aspects of the tumour. Tumour neovascularisation, a hallmark of glioblastoma progression, can be visualised by perfusion MRI. Current perfusion MRI techniques rely on leakage from vessels and do not accurately demonstrate microvasculature.
Vessel Architectural Imaging (VAI) is a novel perfusion MRI technique which can acquire a plethora of additional perfusion parameters, such as oxygenation and vessel diameter. The practicability and accuracy of VAI for differentiating treatment effects from tumor progression in glioblastoma treatment evaluation has not been studied before.
This study aims to establish the practicability and diagnostic accuracy of VAI-MRI in treatment evaluation of glioblastoma.
Doel van het onderzoek
Can vessel
Onderzoeksopzet
Ten treated glioblastoma patients with a new enhancing lesion on conventional follow-up MRI will undergo VAI-MRI. The definite diagnosis will be made radiologically according to the appropriate guidelines (RANO criteria).
Onderzoeksproduct en/of interventie
n/a
Algemeen / deelnemers
Bart Dijken, van
Hanzeplein 1, P.O. Box 30.001
Groningen
The Netherlands
b.r.j.van.dijken@umcg.nl
Wetenschappers
Bart Dijken, van
Hanzeplein 1, P.O. Box 30.001
Groningen
The Netherlands
b.r.j.van.dijken@umcg.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Histological confirmed glioblastoma after standard treatment
- New contrast enhancing lesion on follow-up MRI
- Written informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Minors (<18 years)
- Residual enhancement on post-operative MRI
- History of previous new enhancing lesion on follow-up MRI
- Treatment different than standard treatment
- Contraindication for MRI (ferromagnetic material in body, pregnancy, claustrophobia)
Opzet
Deelname
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In overige registers
Register | ID |
---|---|
NTR-new | NL6859 |
NTR-old | NTR7037 |
Ander register | Universitair Medisch Centrum Groningen : ABR65208 |